Schütte M, Diadori A, Wang C, Wolosin J M
Department of Ophthalmology and Physiology, Mount Sinai School of Medicine, New York, NY 10029-6574, USA.
Invest Ophthalmol Vis Sci. 1996 Jan;37(1):212-20.
Both nonpigmented epithelia (NPE) and pigmented epithelia (PE) of the ciliary body are thought to participate in the formation of aqueous humor and its pharmacologic regulation. The aim of this study was to identify the similarities and differences in intracellular Ca2+ ([Ca2+]i) changes in each of the two layers in response to adrenergic and cholinergic inputs.
Incubation of the Dutch belted rabbit ciliary body (CB) in low-[Ca2+] solution was used to induce the functional dissociation of the NPE and PE layers from each other. These layers or the intact undissociated CB were loaded with the fluorescent Ca2+ indicator fura-2 and mounted in superfusion chambers for fluorometric measurement of [Ca2+]i.
In the NPE of the intact CB epithelium or in the isolated NPE, 10 microM acetylcholine (ACh), 1 microM brimonidine (UK 14304), or 1 microM epinephrine each elicited minimal rises in [Ca2+]i. On the other hand, the combination of either adrenergic drug with ACh resulted in large mobilizations of this cation. The alpha 1-adrenergic agonist phenylephrine was unable to induce Ca2+ mobilization in the isolated NPE and failed to do so in 10 of 12 intact CB specimens. In the isolated PE, both epinephrine and phenylephrine elicited substantial similar [Ca2+]i increases, ACh induced a smaller and slower rise, and the response to its combination with either adrenergic drug was essentially additive. UK 14304 (+/- ACh) had no measurable effect in these cells.
Each layer of the CBE exhibits distinct alpha-adrenergic control mechanisms. The NPE contains an alpha 2-adrenergic mechanism highly dependent on the cholinergic tone. The PE, in contrast, contains an alpha 1-adrenergic pathway that operates independently of cholinergic input. This segregation of mechanisms provides a basis for highly complex regulatory responses in the intact, syncytially organized ciliary body epithelium.
睫状体的无色素上皮(NPE)和色素上皮(PE)均被认为参与房水的形成及其药理调节。本研究的目的是确定两层细胞对肾上腺素能和胆碱能输入的细胞内Ca2+([Ca2+]i)变化的异同。
将荷兰带兔睫状体(CB)置于低[Ca2+]溶液中孵育,以诱导NPE和PE层彼此功能分离。这些层或完整未分离的CB用荧光Ca2+指示剂fura-2加载,并安装在灌流室中用于荧光测量[Ca2+]i。
在完整CB上皮的NPE或分离的NPE中,10μM乙酰胆碱(ACh)、1μM溴莫尼定(UK 14304)或1μM肾上腺素各自引起[Ca2+]i的最小升高。另一方面,任何一种肾上腺素能药物与ACh的组合都会导致该阳离子的大量动员。α1-肾上腺素能激动剂去氧肾上腺素在分离的NPE中不能诱导Ca2+动员,并且在12个完整CB标本中的10个中也未能诱导。在分离的PE中,肾上腺素和去氧肾上腺素均引起[Ca2+]i的显著相似升高,ACh诱导的升高较小且较慢,并且其与任何一种肾上腺素能药物组合的反应基本上是相加的。UK 14304(±ACh)在这些细胞中没有可测量的作用。
睫状体上皮的每一层都表现出不同的α-肾上腺素能控制机制。NPE含有高度依赖胆碱能张力的α2-肾上腺素能机制。相比之下,PE含有独立于胆碱能输入起作用的α1-肾上腺素能途径。这种机制的分离为完整的、合胞体组织的睫状体上皮中高度复杂的调节反应提供了基础。